Regulating the Third Metal to Design and Engineer Multilayered NiFeM (M: Co, Mn, and Cu) Nanofoam Anode Catalysts for Anion‐Exchange Membrane Water Electrolyzers

Author:

Yang Xiaoxuan1,Liang Jiashun1,Shi Qiurong1,Zachman Michael J.2,Kabir Sadia3,Liang Junwu4,Zhu Jing5,Slenker Benjamin1,Pupucevski Max13,Macauley Natalia3,Kropf A. Jeremy6,Zeng Hao7,Strasser Derek3,Myers Deborah J.6,Xu Hui3,Zeng Zhenhua8,Yan Yushan9,Wu Gang1ORCID

Affiliation:

1. Department of Chemical and Biological Engineering University at Buffalo The State University of New York Buffalo NY 14260 USA

2. Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge TN 37831 USA

3. Giner Inc. Newton MA 02466 USA

4. Optoelectronic Information Research Center School of Physics and Telecommunication Engineering Yulin Normal University Yulin Guangxi 537000 China

5. Department of Materials Science and Engineering National University of Singapore Singapore 117574 Singapore

6. Chemical Sciences and Engineering Division Argonne National Laboratory Lemont IL 60439 USA

7. Department of Physics University at Buffalo The State University of New York Buffalo NY 14260 USA

8. Davidson School of Chemical Engineering Purdue University West Lafayette IN 47907 USA

9. Department of Chemical and Biomolecular Engineering Center for Catalytic Science and Technology University of Delaware Newark DE 19716 USA

Abstract

AbstractAlkaline anion‐exchange membrane water electrolyzers (AEMWEs) for green hydrogen production have received intensive attention due to their feasibility of using earth‐abundant platinum group metal (PGM)‐free catalysts. Herein, the third metal is incorporated into NiFe‐based catalysts to regulate their electronic structures and morphologies, aiming to achieve sufficient oxygen evolution reaction (OER) activity and performance in AEMWEs. The ternary NiFeM (M: Cu, Co, or Mn) catalysts are featured with multiple layered structures and nanofoam network morphologies, consisting of highly OER‐active amorphous Ni‐rich oxide shells and electrically conductive metallic alloy cores. The physical and electronic perturbations to the NiFe induced by a third element lead to a fine‐tuning of the redox ability of the metal sites at the reaction centers, which breaks the scaling relationship between OH* and O* intermediates at the reaction centers. Thus, the unique structural configuration and electronic regulation simultaneously benefit catalytic activity and performance improvements. These NiFeM nanofoam catalysts demonstrated promising anode performance in actual AEMWEs, comparable to the IrO2 reference, especially at high current densities. Notably, using various electrolytes (e.g., KOH solution or pure water) for AEMWEs exhibited a different performance trend among studied NiFeM catalysts, likely due to dynamic changes of catalysts under various OER environments.

Funder

U.S. Department of Energy

Hydrogen and Fuel Cell Technologies Office

Publisher

Wiley

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